Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g45760 | A01 | 30518111 | C | T | missense_variant | MODERATE | c.1321G>A|p.Glu441Lys |
S200 S261 S274 S303 |
2 | BAA01g45760 | A01 | 30518653 | G | A | splice_region_variant&intron_variant | LOW | c.1071+8C>T| |
S60 |
3 | BAA01g45760 | A01 | 30520189 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.137-1G>A| |
S233 |
4 | BAA01g45760 | A01 | 30520270 | C | T | splice_donor_variant&intron_variant | HIGH | c.136+1G>A| |
S32 |
5 | BAA01g45760 | A01 | 30520432 | G | A | upstream_gene_variant | MODIFIER | c.-26C>T| |
S87 |
6 | BAA01g45760 | A01 | 30520597 | G | A | upstream_gene_variant | MODIFIER | c.-191C>T| |
S202 |
7 | BAA01g45760 | A01 | 30520732 | C | T | upstream_gene_variant | MODIFIER | c.-326G>A| |
S4 |
8 | BAA01g45760 | A01 | 30523065 | C | T | upstream_gene_variant | MODIFIER | c.-2659G>A| |
S64 |
9 | BAA01g45760 | A01 | 30523264 | G | A | upstream_gene_variant | MODIFIER | c.-2858C>T| |
S262 |
10 | BAA01g45760 | A01 | 30524165 | C | T | upstream_gene_variant | MODIFIER | c.-3759G>A| |
S219 |